GB1569311A - Process for producing metallized pellets from raw pellets - Google Patents
Process for producing metallized pellets from raw pellets Download PDFInfo
- Publication number
- GB1569311A GB1569311A GB3218/76A GB321876A GB1569311A GB 1569311 A GB1569311 A GB 1569311A GB 3218/76 A GB3218/76 A GB 3218/76A GB 321876 A GB321876 A GB 321876A GB 1569311 A GB1569311 A GB 1569311A
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- GB
- United Kingdom
- Prior art keywords
- pellets
- kiln
- temperature
- raw
- air
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
- C21B13/08—Making spongy iron or liquid steel, by direct processes in rotary furnaces
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Muffle Furnaces And Rotary Kilns (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
(54) A PROCESS FOR PRODUCING METALLIZED PELLETS
FROM RAW PELLETS
(71) We, SUMITOMO METAL INDUSTRIES LTD., a Japanese body corporate of
No. 15, 5-chome, Kitahama, Higashi-ku, Osaka, Japan, and SUMITOMO HEAVY
INDUSTRIES, LTD., a Japanese body corporate of 2-1, Ohtemachi 2 Chome, Chiyoda-ku, Tokyo, 100, Japan, do hereby declare the invention, for which we pray that a
patent may be granted to us, and the method by which it is to be performed, to be
particularly described in and by the following statement::
This invention relates to a process for reducing raw pellets containing metal oxides, such
as iron oxide, zinc oxide, etc. to metallized pellets having a high metal content in a rotary
kiln without forming powder of the pellets in the kiln or without ring formation in the kiln,
and more particularly relates to a process for producing the metallized pellets by blowing air
or spraying water into the portion near the charge end of the kiln in order to obtain
metallized pellets.
It is desirable to recycle the iron-containing dust exhausted from blast furnace, converter
furnace, electric furnace and open hearth furnace, etc. into the blast furnace in order to
recover iron therefrom and to prevent environmental pollution. Furthermore, since the
dust has about 50% by weight of iron, the reuse of the dust is desirable from the point of
view of saving material resources.
The term "raw pellets" in the specification and the claims means pellets obtained by iletizing the iron works dust exhausted from blast furnace, electric furnace, converter mace and/or open hearth furnace, etc. or a mixture of the dusts and optionally carbon
source, such as coal or coke. The term "iron-containing dust" in the specification and the
claims means powdery materials withdrawn as-by-products from blast furnace, electric
furnace, converter furnace or open hearth furnace, etc. for smelting a metal or for making a
metal. The term "metallized pellets" in the specification and the claims means pellets with a
high concentration of iron obtained by chemically reducing said raw pellets.
It was known that pellets having a high metallic iron content can be prepared by reducing
the raw pellets in a rotary kiln. One process for reducing the raw pellets in the kiln
comprises the step of charging the pellets into the kiln, and the step of reducing the metal
oxides contained in the raw pellets at a high temperature and at the same time volatilizing
other metals, particularly zinc. The reduction of the metal oxides with carbon is represented
by the following equation:
MO + C o M + CO
wherein M is a metal element.
Coal or coke may be mixed with the dust before pelletizing it. When the iron-containing
dust has a high carbon content, it may be unnecessary to mix the coal or coke with the dust.
The dust can be generally preheated at a temperature of 400"C or less so that carbon in
pellets or metal oxide may not be burnt. Particularly, dust containing wustite or metallic
iron can be preheated at a temperature only below 200"C, because wustite or metallic iron is likely to be oxidized and subjected to exothermic reaction temperature above 200"C.
Therefore, preferably the iron-containing dust is preheated at a temperature below 200"C.
One prior process for reducing the raw pellets to the metallized pellets has the following "disadvantages:
When the raw pellets are introduced into a rotary kiln, the raw pellets are ground during their passage through the kiln and as a result a ring is formed in the kiln. Therefore, the continuous operation in the rotary kiln is impossible. The cause of the ring formation has not been disclosed in the prior art.
Figure 1 is a graph showing the relationship between the zinc content in the resulting metallized pellets and metallization ratio of iron;
Figure 2 is a graph showing the relationship between the zinc content in the resulting metallized pellets and the temperature of as exhausted from the charge end of kiln;
Figure 3 is a graph showing the relationship between the ratio of At O/At F e and the crushing strength of the pellets at each reducing stage; Figure 4 is a graph showing the relationship between the zinc content in the resulting metallized pellets and the temperature of gas exhausted from the charge end of kiln;
Figure 5 is flow sheet showing the stages in reducing the raw pellets; and
Figure 6 is a graph showing the distribution of temperature in the kiln according to this invention and the distribution of temperature in the kiln in case of neither blowing air nor spraying water.
The inventors of the present invention have carried out a variety of research in order to prevent the ring formation.
When the raw pellets are heated in a rotary kiln at an elevated temperature, ferric oxide (foe203) contained in the raw pellets is reduced to metallic iron via Fe3O4 and FeO. For example, the raw pellets having the components shown in Table 1 were heated in a rotary kiln 6.57 m long and 0.46 m internal diameter to reduce iron oxide to metallic iron and to reduce zinc oxide and volatilize the resulting metallic zinc.
TABLE 1
Components of raw pellets (%) Awl203 SiO2 Zn C Metallic Fe Fe203 FeO CaO
1.2 2.7 0.51 13.1 2.6 50.3 16.2 3.6
This pellets contain 50.4% of total Fe.
We determined the zinc content in the resulting metallized pellets and the metallization ratio (the proportion of metallic iron to total iron) in the pellets. The above experiments were repeated many times using pellets having different components. The relationship between the zinc content in the resulting metallized pellets and metallization ratio of iron is
shown in Figure 1.
It may be stated from Figure 1 that the metallization ratio of iron oxide has a great influence on the zinc content in the metallized pellets.
Raw pellets having the components mentioned above were reduced in a rotary kiln as mentioned above at a speed of rotation of 0.33 rpm. The reducing procedures were carried out many times at the different temperature of gas exhausted from the charge end of the
kiln. The relationship between between the zinc content in the resulting metallized pellets and the temperatures is shown in Figure 2. In view of the conditions under which the resulting metallized pellets are used, it tends to be necessary to keep the zinc content of the metallized pellets to less than 0.1% by weight. From the results of Figure 2, the temperature of exhaust gas tends to be more than about 520"C in order to obtain pellets
having a zinc content below 0.1% by weight.The above experiments were carried out without blowing air or spraying water into the portion near the charge end of the kiln.
Therefore, a ring was formed at a distance of 2 meter from the discharge end of kiln. As a result, it was found that a continuous operation of rotary kiln was impossibnle over more
than 10 - 12 hours.
The ratio of the number of oxygen atoms bonded to iron atoms in the raw pellets to the number of iron atoms in the raw pellets (hereinunder abbreviated as At O/At Fe) decreases as the reduction of the raw pellets proceeds. The inventors of the present invention carried
out a variety of experiments for investigating the transition of the crushing strength of the pellets. The results are shown in Figure 3. From the result, it is understood that the crushing strength of the pellet is extremely low at the magnetite stage. It has been found that when the temperature of pellets is rapidly raised at the magnetite state which magnetite is formed, the crushing strength of the pellets is weak, and in other words when the temperature is rapidly raised during the magnetite stage the pellets are very likely to powder and a ring formation is very likely to be formed in the rotary kiln.
We have found that the rate of raising the temperature of the raw pellets in the range between about 600"C - about 800"C has an influence on the formation of the ring formation, that is when the raw pellets are rapidly heated in said range, the ring formation tends to occur.
Considering the above discovery and the above experimental results, we have carried out research on the process for reducing the raw pellets in the rotary kiln without ring formation.
Raw pellets having the components shown in Table 1 were reduced in a rotary kiln at a speed of rotation of 0.25 rpm. The reducing procedures were carried out at the different temperatures of exhaust gas many times. The relationship between the zinc content in the resulting metallized pellets and the temperature is shown in Figure 4. The retention time of the raw pellets in case of the rotation of 0.25 rpm is longer by four-third than the retention time of the raw pellets in case of the rotation of 0.33 rpm. From the results of Figure 4, the temperature of gas exhausted from the charge end of kiln may be as low as about 420"C in order to obtain pellets having a zinc content below 0.1% by weight. We have found that when the residence time of the raw pellets was lengthened the reducing procedure could be continued without any trouble, that is ring formation.However, when the rotary kiln is operated at slow speed of rotation, this tends to be costly because it lowers the productivity per unit volume of the rotary kiln.
Furthermore, when a longer rotary kiln is used, it is expected that the temperature near the charge end will be lowered to such an extent that the ring may not be formed in the kiln.
However, this tends to be also costly, because it lowers the productivity per unit volume of the rotary kiln.
We have found that when air or water in a spray state is introduced into the portion near the charge end of the kiln, too rapid heating of the raw pellets in the kiln can be avoided in the range between from about 600"C to about 800"C.
Therefore, it is an object of this invention to provide a process for reducing the raw pellets prepared from the iron-containing dust exhausted from the iron plants to metallized pellets in a rotary kiln without ring formation in the kiln.
Another object of this invention is to provide a process for reducing the raw pellets with the same productivity per unit volume of rotary kiln as the prior process for reducing the pellets.
This invention relates to a process for chemically reducing raw pellets to metallized pellets which comprises charging the raw pellets containing an appropriate amount of carbon source into a rotary kiln, and reducing the metal oxides contained in the raw pellets with the carbon, characterized in that air is blown or water is sprayed either into the region of the kiln which is near the charge end, and in which region the combustion does not occur, or the region of the kiln in which combusion occurs, whereby the introduction of air or water in a spray state lowers the temperature of the region into which it is introduced and
reduces the heating slope of the raw pellets in the temperature range of from 600"C to
8000C.
This invention is further illustrated by the non-limitative drawing. Referring to Figure 5,
raw pellets containing carbon are charged into entrance 3 for pellets of rotary kiln and are
moved to exit 4 for pellets. Fuel oil is fed through burner 8. Air for combustion of carbon
monoxide is fed into kiln 1 through feeding pipes 5, and air or water in the form of a spray is
fed into kiln 1 through inlet 6. Kiln 1 is shown equipped with a single inlet 6 but it may, if
desired, be equipped with several inlets. When air or water in a spray state is fed into the
portion near charge end 7 or kiln 1 through pipe 6, the temperature of the portion is
lowered, whereby too rapid heating of the pellets 2 near charge end 7 can be avoided. Metal
oxides contained in the pellets react with carbon to form metal and carbon monoxide. The
carbon monoxide is burnt to form carbon dioxide.The temperature of the combustion
portion of kiln 1 generally is more than 950"C. During the reducing reaction, zinc is
vaporized. Before introducing the raw pellets into kiln 1, coal or coke may be added to the
pellets as a reducing agent.
The raw pellets may be predried to a temperature below 400"C so that carbon contained
therein is not burnt before introducing them in the kiln.
Figure 6 shows the distribution of temperature in the kiln. Curve A is the distribution of
temperature of gas in case of not introducing air or water near the charge end. Curve B is
the distribution of temperature of gas in case of introducing air or water in a spray state near
the charge end. Curve A' is the distribution of temperature of the raw pellets in case of not
introducing air or water near the charge end. Curve B' is the distribution of the temperature
of the raw pellets in case of introducing air or water in a spray state near the charge end.
The temperature of the raw pellets in the charge end of the kiln was 20"C. In all cases the
rotary kiln was operated at the same rotational frequency. It is apparent from Figure 6 that
when air is blown or water is sprayed near the charge end, the heating curve of the raw
pellets in the range between from about 600"C to about 800"C is less steep than when
neither air is blown, nor water is sprayed near the charge end.
In the example shown in Figure 6, when air or water is introduced into the portion near the charge end, the atmospheric temperature of the charge end is lower by about 1700C than when no air or water is introduced into said portion. Therefore, there is little possibility of breakdown of the pellets by heat strain. However, the atmospheric temperature of the charge end in case of introducing air or water into said portion can be controlled by adjusting the amount of air introduced into said portion. Furthermore, specific heat of the pellets is higher than that of the gas, so the temperature of the pellets is always lower than the temperature of gas.The reason why the temperature of gas in the combustion area in the process according to the present invention is higher than the temperature of gas in the prior process is that in the present invention all carbon monoxide is burnt in the portion between the discharge end and the center of the kiln.
In one embodiment of the invention air or water in a spray state for cooling is added to the region of the kiln which is near the charge end, where combustion does not occur. In other words, air or water in a spray state is added to the portion of the kiln so that introduction of air or water does not promote the heating of the portion, but cools the portion.
In an alternative embodiment, air or water in a spray state may be introduced into the portion at which combustion occurs, provided that introduction of air or water in a spraying state can lower the temperature of the portion.
The distance from the charge end at which the air or the water in a spray state is introduced and the amount of air or water introduced are interdependent variables.
However, air or water in a spray state is introduced into the portion near the charge end so as to insure that the heating slope of the raw pellets becomes lower in the range between about 600"C and about 800"C. It is desirable that the air or water in a spray state is introduced into a region of the kiln in the first 3/7 of the entire length of the kiln, as measured from the charge end thereof.
The amount of air or water in a spray state introduced can be easily decided by those skilled in the art.
The amount of gas for combustion feed and the rotational frequency of the kiln are not critical.
According to the present invention using a rotary kiln, metallized pellets having a zinc content below 0.1% by weight and a high metallization ratio can be prepared from raw pellets with the same productivity per unit volume of rotary kiln as the prior process and without ring formation in the kiln.
According to the present invention, the rotary kiln can be operated at the same rate of rotation as in the prior process.
The present invention is further illustrated by the following Example. However, this invention should not be limited by this Example. The percent and parts in the Example are based on weight unless otherwise specified.
Example The raw pellets having the components shown in foregoing Table 1 were heated in a rotary kiln 6.57 m long and 0.46 m internal diameter to reduce iron oxide to metallic iron and to reduce zinc oxide and volatilize the resulting metallic zinc. The kiln was equipped with shell-fan, thermometer, coal-charging means, gas-analyzing means and dust-collecting means. Air for cooling was blown at the distance of 2 m from the charge end of the kiln. The conditions of the experiment carried out were shown in Table 2.
The similar procedures of Example 1 were repeated except that air for cooling was not blown as control tests. The conditions of the control tests carried out were also shown. The results are shown in Table 2.
TABLE 2
Example Control Control
1 test 1 test 2
Temperature of pellets charged ( C) 20 20 20
Amount of pellets charged (Kg)hr) 50 50 35
Speed of rotation of the kiln (rpm) 1/3 1/3 1/4
Retention time of the pellets in 290 290 370 the kiln (min.)
Amount of fuel oil used (Kg)hr) 4.0 4.0 4.0
Temperature of exhaust gas ("C) 400 570 420
Temperature of pellets 1120 1120 1110 discharged from kiln ("C) Whether ring is formed No Yes No
Time for which the continuous more 10 more operation was possible (hr) than than
200 200
Whether air for cooling was blown Yes No No
Metallization ratio of iron (%) 94 94 93
Zinc content in reduced pellets (%) 0.04 0.06 0.06
In control test 1, a ring was formed in the kiln. Therefore, continuous operation of the kiln was impossible.In control test 2, the rotary kiln was operated at a slow speed of rotation. This tends to be costly, because it lowers the productivity per unit volume of the rotary kiln.
WHAT WE CLAIM IS:
1. A process for reducing raw pellets, prepared from iron-containing dust exhausted from an iron plant, to metallized pellets having a high metallic iron content which comprises charging the raw pellets containing an appropriate amount of a carbon source into a rotary kiln, and heating to reduce the metal oxides contained in the raw pellets with the carbon, wherein cooling air or water in the form of a spray is introduced into either a region of the kiln which is near the charge end and in which combustion does not occur, or region of the kiln in which combustion occurs, whereby the introduction of air or water in a spray state lowers the temperature of the region into which it is introduced and reduces the heating sloe of the raw pellets in the temperature range of from 600"C to 800"C.
2. A process as claimed in claim 1 wherein the air or the water in a spray state is introduced into a region of the kiln in the first 3/7 of the entire length of the kiln, as measured from the charge end thereof.
3. A process as claimed in any one of claims 1 or 2, wherein the raw pellets contain about 0.5 Per cent by weight of zinc and the resulting metallized pellets contain less than 0.1 per cent by weight of zinc.
4. A process as claimed in claim 1 and substantially as hereinbefore described with reference to the Examples.
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (4)
1 test 1 test 2
Temperature of pellets charged ( C) 20 20 20
Amount of pellets charged (Kg)hr) 50 50 35
Speed of rotation of the kiln (rpm) 1/3 1/3 1/4
Retention time of the pellets in 290 290 370 the kiln (min.)
Amount of fuel oil used (Kg)hr) 4.0 4.0 4.0
Temperature of exhaust gas ("C) 400 570 420
Temperature of pellets 1120 1120 1110 discharged from kiln ("C) Whether ring is formed No Yes No
Time for which the continuous more 10 more operation was possible (hr) than than
200 200
Whether air for cooling was blown Yes No No
Metallization ratio of iron (%) 94 94 93
Zinc content in reduced pellets (%) 0.04 0.06 0.06
In control test 1, a ring was formed in the kiln. Therefore, continuous operation of the kiln was impossible.In control test 2, the rotary kiln was operated at a slow speed of rotation. This tends to be costly, because it lowers the productivity per unit volume of the rotary kiln.
WHAT WE CLAIM IS:
1. A process for reducing raw pellets, prepared from iron-containing dust exhausted from an iron plant, to metallized pellets having a high metallic iron content which comprises charging the raw pellets containing an appropriate amount of a carbon source into a rotary kiln, and heating to reduce the metal oxides contained in the raw pellets with the carbon, wherein cooling air or water in the form of a spray is introduced into either a region of the kiln which is near the charge end and in which combustion does not occur, or region of the kiln in which combustion occurs, whereby the introduction of air or water in a spray state lowers the temperature of the region into which it is introduced and reduces the heating sloe of the raw pellets in the temperature range of from 600"C to 800"C.
2. A process as claimed in claim 1 wherein the air or the water in a spray state is introduced into a region of the kiln in the first 3/7 of the entire length of the kiln, as measured from the charge end thereof.
3. A process as claimed in any one of claims 1 or 2, wherein the raw pellets contain about 0.5 Per cent by weight of zinc and the resulting metallized pellets contain less than 0.1 per cent by weight of zinc.
4. A process as claimed in claim 1 and substantially as hereinbefore described with reference to the Examples.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3218/76A GB1569311A (en) | 1977-01-20 | 1977-01-20 | Process for producing metallized pellets from raw pellets |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3218/76A GB1569311A (en) | 1977-01-20 | 1977-01-20 | Process for producing metallized pellets from raw pellets |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1569311A true GB1569311A (en) | 1980-06-11 |
Family
ID=9754194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3218/76A Expired GB1569311A (en) | 1977-01-20 | 1977-01-20 | Process for producing metallized pellets from raw pellets |
Country Status (1)
Country | Link |
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GB (1) | GB1569311A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11479832B2 (en) | 2016-04-22 | 2022-10-25 | Sumitomo Metal Mining Co., Ltd. | Method for smelting oxide ore |
US11608543B2 (en) * | 2016-04-27 | 2023-03-21 | Sumitomo Metal Mining Co., Ltd. | Oxide ore smelting method |
-
1977
- 1977-01-20 GB GB3218/76A patent/GB1569311A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11479832B2 (en) | 2016-04-22 | 2022-10-25 | Sumitomo Metal Mining Co., Ltd. | Method for smelting oxide ore |
US11608543B2 (en) * | 2016-04-27 | 2023-03-21 | Sumitomo Metal Mining Co., Ltd. | Oxide ore smelting method |
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Legal Events
Date | Code | Title | Description |
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PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |